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CompletedNCT00216632

Switching from olanzapine to long-acting risperidone in stable schizophrenia

About this title

A Study of Treatment Success in Changing From Olanzapine to Long-acting Injectable Risperidone (RISPERDAL® CONSTA™)

Read the official source — NCT00216632
Medication studyAges 18+
The study in practice

Understand this study

Who was this study for?

Listed age limits: from 18 years.

Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Study clarity

Study information

Study start dateMarch 2005
Recruitment status
Completed
Enrollment listed in the registry
99
Sponsor
Janssen Pharmaceutica N.V., Belgium
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug
Study phase
Phase 4Usually happens after approval, to monitor real-world use, safety, and longer-term outcomes.
Locations
Not clearly listed
Age range
Over 18 Years
Official registry ID
NCT00216632
Official title
Show the full official title

Treatment Success in Patients Requiring Treatment Change From Olanzapine to Risperidone Long Acting Injectable (TRESOR)

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Recruitment & locations

Completed

Locations not listed

FAQ

Questions about this study

Who is behind this study?

The study sponsor is Janssen Pharmaceutica N.V., Belgium.

Did this study involve medication?

Yes. The study involved medication, including risperidone.

Who was this study for?

Listed age limits: from 18 years.

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